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人类肾硫酸钠共转运体(SLC13A1;hNaSi-1)的cDNA和基因:结构、染色体定位及功能特性

The human renal sodium sulfate cotransporter (SLC13A1; hNaSi-1) cDNA and gene: organization, chromosomal localization, and functional characterization.

作者信息

Lee A, Beck L, Markovich D

机构信息

Department of Physiology and Pharmacology, University of Queensland, Brisbane, Queensland, 4072, Australia.

出版信息

Genomics. 2000 Dec 15;70(3):354-63. doi: 10.1006/geno.2000.6404.

Abstract

Sulfate plays an essential role during growth, development, bone/cartilage formation, and cellular metabolism. In this study, we have determined the structure of the human Na+-sulfate cotransporter (hNaSi-1) cDNA (Human Genome Nomenclature Committee-approved symbol SLC13A1) and gene (NAS1). hNaSi-1 encodes a protein of 595 amino acids with 13 putative transmembrane domains. hNaSi-1 mRNA expression was exclusive to the human kidney. Expression of hNaSi-1 protein in Xenopus oocytes demonstrated a high-affinity Na+-sulfate cotransporter that was inhibited by selenate, thiosulfate, molybdate, tungstate, citrate, and succinate. Antisense inhibition experiments suggest hNaSi-1 to represent the major Na+-sulfate cotransporter in the human kidney. NAS1 was localized on human chromosome 7, mapped to 7q31-q32, near the sulfate transporter genes, DRA and SUT-1. The NAS1 gene contains 15 exons, spanning over 83 kb in length. Knowledge of the structure, function, and chromosomal localization of hNaSi-1 will permit the screening of NAS1 mutations in humans with disorders in renal sulfate reabsorption and homeostasis.

摘要

硫酸盐在生长、发育、骨骼/软骨形成以及细胞代谢过程中发挥着重要作用。在本研究中,我们确定了人类钠离子-硫酸盐共转运蛋白(hNaSi-1)的cDNA(人类基因组命名委员会批准的符号为SLC13A1)和基因(NAS1)的结构。hNaSi-1编码一个含有595个氨基酸的蛋白质,具有13个推定的跨膜结构域。hNaSi-1 mRNA表达仅在人类肾脏中出现。hNaSi-1蛋白在非洲爪蟾卵母细胞中的表达证明其是一种高亲和力的钠离子-硫酸盐共转运蛋白,可被硒酸盐、硫代硫酸盐、钼酸盐、钨酸盐、柠檬酸盐和琥珀酸盐抑制。反义抑制实验表明hNaSi-1是人类肾脏中主要的钠离子-硫酸盐共转运蛋白。NAS1定位于人类7号染色体,定位于7q31-q32,靠近硫酸盐转运蛋白基因DRA和SUT-1。NAS1基因包含15个外显子,长度超过83 kb。了解hNaSi-1的结构、功能和染色体定位将有助于筛查患有肾脏硫酸盐重吸收和稳态紊乱的人类中的NAS1突变。

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